Light-selective particles, related methods and related applications

ABSTRACT

A method for preparing a light sensitive particle that uses at least one metal precursor material and at least one dopant precursor material mixed in solution absent a surfactant. Upon an optional adjustment of pH to about 3 to about 6, a light-sensitive particle comprising a metal-dopant material may be formed and separated from the solution. The light-sensitive particle may comprise a Q-dot particle. Also described are the particles themselves.

CROSS-REFERENCE TO RELATED APPLICATION

This application relates to, and derives priority from, U.S. ProvisionalPatent Application Ser. No. 62/042,299, filed Aug. 27, 2014 and titled“Fluorescent Gels and Methods of Making Fluorescent Gels,” the contentof which is incorporated herein fully by reference.

GOVERNMENT SUPPORT

The embodiments as described herein, and the inventions as claimedherein, were made with United States Government support underContract/Grant No. 1159500, awarded by United States National ScienceFoundation. The United States Government has rights in the invention asclaimed herein.

BACKGROUND

1. Field

Embodiments relate generally to light-selective particles and methodsfor preparing the light-selective particles. More particularly,embodiments relate to light-selective particles with enhancedperformance and methods for preparing the light-selective particles withthe enhanced performance.

2. Description of the Related Art

Light-selective particles, such as but not limited to light-emittingparticles, and more particularly such as but not limited to fluorescentlight-emitting particles which are intended to include quantum dotparticles (i.e., Q-dot particles), find use in several scientificallyadvanced technical applications, including but not limited opticalcomputing applications and molecular biology applications. Within thecontext of these applications, the light-selective particles may beincluded and used within devices such as but not limited to photovoltaicdevices, light-emitting diode devices and photodetector devices.

While light-selective particles, including in particular fluorescentlight-emitting particles such as Q-dot particles, are key enablingcomponents within several scientifically advanced technicalapplications, light-selective particles are nonetheless not entirelywithout problems. In that regard, it is often difficult to preparelight-selective particles, and in particular fluorescent light-emittingparticles such as Q-dot particles, with enhanced purity to ensureoptimal operation of apparatus and components predicated upon use ofthose light-selective particles.

Thus, desirable within the light-selective particle art are enhancedperformance light-selective particles and methods for preparing theenhanced performance light-selective particles.

SUMMARY

Embodiments include light-selective particles such as but not limited tofluorescent light-emitting particles, and methods for preparing thelight-sensitive particles such as but not limited to the fluorescentlight-emitting particles. In a particular embodiment, light-selectivefluorescent light-emitting particle compositions in accordance with theembodiments are 100% free of a surfactant, as compared with otherwiseknown fluorescent light-emitting particle compositions prepared using atleast one surfactant, where removal of all the surfactant residue postlight-emitting particle preparation (i.e., synthesis) may otherwiseprove to be quite difficult. Surfactant materials when used forfabricating light-sensitive particles serve as emulsifying agents thatlower a surface tension between an aqueous phase and an organic phase ofa synthesis mixture or solution that is used for preparing thelight-sensitive particles. This particular absence of a surfactantresidue provides a light-emitting particle of greater light emittingintensity insofar as surfactant residue induced quenching and absorptionis eliminated. In addition, such an absence of a surfactant residue alsoprovides light-sensitive particles that are more light-sensitive, as isthe need for light-sensitive particle applications.

A particular method in accordance with the embodiments (i.e., a sol-gelmethod that is alternatively referred to as a “sol-glow” method thatyields “sol-glow” particles which may comprise fluorescent gelparticles) provides a water based one-pot chemical synthesis method thatis rapid and relies on simple mixing steps. This particular method andthe related resulting fluorescent light-emitting particles are ofparticular interest within the context of electronic and optoelectronicapplications. For agriculture industry applications, light-emittingparticles can serve as a plant nutrient fertilizer and also as anantimicrobial agent that is intended to protect crops from bacterial andother microbial infections. In general the sol-gel method in accordancewith the embodiments is readily extendable to various inorganic lightsensitive semiconductor materials which may be subsequently coated withvarious organic light sensitive dye materials (i.e., fluorescent dyematerials) using chemical reaction methodology as is otherwise generallyknown in the particle preparation art.

Methodological embodiments in accordance with the present disclosure caninclude mixing at least one first water soluble core metal precursormaterial (e.g., at least one water soluble metal compound such as butnot limited to cadmium acetate, zinc acetate, manganese acetate, or thelike) with at least one first water soluble dopant precursor material(e.g., sodium sulfide or the like) to form a doped metal core material.By adding a specific quantity of at least one second water soluble shellmetal precursor material and at least one second water soluble dopantprecursor material, a core-shell light-emitting particle may be formedabsent a surfactant residue. Under certain instances of certain specificprecursor material choices a change in pH may additionally be desirableto achieve most efficient production of the resulting core-shelllight-emitting particles. Typically the pH of the final composition maybe adjusted to about 3 to 6 to form the desirable resulting core-shelllight-emitting particles. The process of forming the core-shelllight-emitting particles which are alternatively designated asfluorescent gel particles in accordance with the embodiments issurfactant free (e.g., whereas in comparison surfactants are otherwisegenerally used to form Q-dots and the like), which is distinct incomparison with other processes.

In a particular embodiment, the at least one water soluble first coremetal precursor material, the at least one water soluble first coredopant precursor material, the at least one water soluble second shellmetal precursor material and the at least one water soluble second shelldopant donor precursor material are in the aqueous phase. In aparticular embodiment, the resulting core-shell fluorescent lightemitting particles can be selected from: CdS:Mn/ZnS, ZnS:Mn/ZnS,MnS:Mn/ZnS, or the like, where the foregoing chemical formula areintended as representative of a core-shell (i.e., core: shell)structure. In an embodiment, the formed fluorescent gel particles are100% free of surfactant. Additional fluorescent gel particle preparationdetails are provided in the experimental examples recited below.

The present disclosure describes a surfactant-free method for preparinga metal/dopant based water-dispersible fluorescent gel particle (such asCdS:Mn/ZnS, ZnS:Mn/ZnS and MnS:Mn/ZnS) (analogous terminology isfluorescent quantum dot particle, Q-dot particle). The methodology inaccordance with the embodiments uses a one-pot water based chemicalpreparation and synthesis method that is simple enough to producehigh-quality gel particles in scalable quantity (metric ton scale). Theprocess is rapid and relies on simple mixing steps. Surfactant-free gelparticles are particularly desirable for applications in the electronic,optoelectronic and agriculture industries.

A particular particle in accordance with the embodiments includes atleast one portion that includes a light-selective composition absent asurfactant residue.

A particular method for preparing a particle in accordance with theembodiments includes mixing in an aqueous solution absent a surfactantmaterial at least one metal precursor material and at least one dopantprecursor material to provide a metal-dopant material particle absent asurfactant residue.

Another particular method for preparing a particle in accordance withthe embodiments includes mixing in an aqueous solution absent asurfactant material at least one metal precursor material and at leastone dopant precursor material to provide a metal-dopant materialparticle absent a surfactant residue. This other particular method alsoincludes further reacting the metal-dopant material particle absent thesurfactant residue with an encapsulant precursor material to provide acore-shell encapsulated metal—dopant material particle.

Another particular particle in accordance with the embodiments includesfirst light sensitive area comprising a first light sensitive materialand a second light sensitive area comprising a second light sensitivematerial different than the first light sensitive material.

BRIEF DESCRIPTION OF THE DRAWINGS

The objects, features and advantages of the embodiments are understoodwithin the context of the Detailed Description of the Non-LimitingEmbodiments, as set forth below. The Detailed Description of theNon-Limiting Embodiments is understood within the context of theaccompanying drawings, which form a material part of this disclosurewherein:

FIG. 1A (left) shows room lighting images illustrating surfactant freegel particles on the ft and micro-emulsion surfactant synthesized gelparticles on the right. FIG. 1B (right) shows UV-excitation imageshowing the fluorescence of surfactant free gel particles on the leftand micro-emulsion synthesized gel particles on the right.

FIG. 2A shows three high resolution transmission electron microscopy(HRTEM) images showing 5 nm sized gel particles. The fourth image showsselective area electron diffraction (SAED) image that illustrates thecrystallinity and lattice plane spacings. FIG. 2B shows electrondispersion x-ray (EDX) spectroscopy confirming the particle compositionof ZnS:Mn gel particles on a carbon coated copper grid.

FIG. 3A and FIG. 3B shows fluorescence emission of CdS:Mn/ZnS and ZnS:Mngel particles measured using a NanoLog spectrofluorimeter (SPEX, JobinYvon Horiba) without a neutral density filter. Spectra were collectedfor washed gel particles that were removed from a micro-emulsion andredispersed in water.

FIG. 4A and FIG. 4B show fluorescence activation of CdS:Mn/ZnSsemiconductor material, and increasing intensity with decreasing pH.Fluorescence intensity was measured using the NanoLog spectrofluorimeter(SPEX, Jobin Yvon Horiba) with a neutral density filter. The spectralcurves at 600 nm follow in an inverse order with respect to the legend,with the exception that pH 6.02 is the lowest curve.

FIG. 5A and FIG. 5B show fluorescence activation of ZnS:Mn semiconductormaterial, and increasing intensity with decreasing pH. Fluorescenceintensity was measured using the NanoLog spectrofluorimeter (SPEX, JobinYvon Horiba) with a neutral density filter. The spectral curves at 600nm in increasing intensity correspond with pH 10.26, 6.35, 1.68, 5.37,4.98, 4.68, 4.39, 4.08 and 3.68.

FIG. 6A and FIG. 6B show fluorescence quenching of ZnS:Mn semiconductormaterial with increasing H₂0₂ concentration showing a slow oxidation ofZnS semiconductor material to ZnO. Fluorescence intensity was measuredusing the NanoLog spectrofluorimeter (SPEX, Jobin Yvon Horiba). Aneutral density filter was used only to measure the initial gel particlefluorescence before hydrogen peroxide addition. The spectral curves at600 mn correspond in direct order with respect to the legend.

FIG. 7A and FIG. 7B show fluorescence quenching of ZnS:Mn semiconductormaterial with increasing Quat surfactant volume showing the slow coatingof ZnS:Mn semiconductor material to ZnS:Mn/Quat. A neutral densityfilter was used only to measure the initial gel particle fluorescencebefore Quat addition. The spectral curves at 600 nm in increasingintensity correspond with 10, 20, 5, 50, 100 and zero parts Quat.

FIG. 8 shows 200 ml large scale synthesis of surface modified surfactantfree gel particles showing long term shelf life and water solubility.Sodium salicylate (SS), TEOS (TE), and sodium gluconate (SG) wereincorporated as solubilizing agents.

FIG. 9 Shows UV-visible absorbance of CdS:Mn/ZnS gel particle coatedwith TEOS (silica), sodium salicylate and sodium gluconate was collectedusing a Cary 300 UV-visible spectrophotometer. Respective controls areincluded for comparison. Bare sol-gel particles were dilutedappropriately in order to obtain an absorbance of 0.1 at 350 nm. Coatingagents improve gel particle solubility as noted by the reduced lightdiffraction between bare and coated gel particles. The spectral curvesat 0.4 absorbance from left to right are dark blue, light blue, green,gray, pink, red and brown.

FIG. 10 shows fluorescence emission of CdS:Mn/ZnS semiconductor materialshowing the maturation of the sol-glow particle and Mn²⁺ dopantenvironment as fluorescence increased between Day 1-Day 6. In addition,relative fluorescence emissions for sodium gluconate, sodium salicylate,and TEOS coated gel particles are provided. The spectral curves at 600nm follow inversely with respect to the legend, with the exception thatsodium salicylate is uppermost.

FIG. 11 shows fluorescence emission of ZnS:Mn semiconductor materialshowing the maturation of the gel particle and Mn²⁺ dopant environmentas fluorescence increased between Day 1-Day 6.

FIG. 12A shows Fourier transform infrared (FUR) spectra of bare andcoated fluorescent gel particles. The spectral curves at 3200wavenumbers in increasing intensity correspond with sodium gluconate,bare Q-dot, TEOS and sodium salicylate. FIG. 12B shows chemicalstructures of the coating materials indicted above.

FIG. 13 shows ambient light image of water soluble ZnS:Mn gelnanoparticles (FIG. A) showing (from left to right) glutathion (GSH)coated, N-acetyl cysteine (NAC) coated, sodium gluconate (SG) coated,NAC/GSH co-coated, NAC-fluoresceine isothiocyanate (FllC) coated, andbare uncoated. Same samples showing fluorescence emission under 254 nmexcitation (FIG. B) and 365 nm excitation (FIG. C).

FIG. 14 shows UV visible absorbance spectra of water soluble ZnS gelQ-dots at 326 nm excitation. ZnS bare (blue) at pH 1. ZnS NAC (red,N-acetyl cysteine) at pH 9.26, ZnS SG at pH 5.6 (green, sodiumgluconate), ZnS NAC-FITC at pH 9 (purple, fluoresceine isothiocyanate),ZnS NAC/GSH (light blue, co-coated with NAC and glutathione), and ZnSGSH pH 8 (orange) have all been standardized to 0.1 absorbance at 326 nmusing a CaryWin UV Spectrophotometer. Peak absorbance at 490 nmindicates the presence of FITC on the ZNS NAC-FITC Q-dot. At 200 nm theZnS SG absorbs about 0.85 and the ZnS bare absorbs about 0.38. Theremainder of the ZnS compositions provide extinction of light at about300 nm

FIG. 15 shows peak fluorescence emission of water soluble ZnS gel Q-dotsat 326 nm excitation. ZnS Bare (Blue) at pH 1. ZnS NAC (red, N-acetylcysteine) at pH 9.26, ZnS SG at pH 5.6 (green, sodium gluconate ZnSNAC-FITC at pH 9 (purple, fluoresceine isothiocyanate ZnS NAC/GSH(black, co-coated with NAC and glutathione ZnS GSH pH 8 (orange), and MENAC pH 5.6 (dark blue, ZnS Q-dots prepared in w/o micro emulsion) haveall been standardized to 0.1 absorbance at 326 nm using a CaryWin UVSpectrophotometer. ME NAC included as a comparison example. In order ofdecreasing absorbance at 600 nm is bare, GSH, NAC, NAC-GSH, AC-FITC SGand ME-NAC

FIG. 16 shows fluorescence emission of ZnS NAC-FITC (N-acetyl cysteinelinked fluoresceine isothiocyanate) with 400 nm excitation showing the510 nm emission of FITC confirming the presence of an organic dye on theQ-dot.

FIG. 17 shows dynamic light scattering (DLS) of bare ZnS Q-dotsdispersed in water at neutral pH showing micron-sized particles. AverageZeta potential is 10.77 mV

FIG. 18 shows dynamic light scattering (DLS) of coated ZnS NAC Q-dotssolubilized in water at pH 9.26 showing an average particle size of35.28 nm. Average Zeta potential was −15.87 mV.

FIG. 19 shows dynamic light scattering (DLS) of coated ZnS sodiumgluconate Q-dots solubilized in water at pH 5.6 showing an averageparticle size of 1407 nm. Average Zeta potential was −30.13

FIG. 20 shows dynamic Light Scattering (DLS) of coated ZnS NAC/GSHQ-dots solubilized in water at pH 9.26 showing average particle sizesranging from 8.6 nm to 104 nm.

FIG. 21 shows dynamic light scattering (DLS) of coated ZnS GSH Q-dotssolubilized in water at pH 8 showing an average particle size of 60.80nm.

FIG. 22 shows cytotoxicity assay using Alamar Blue, showing the toxicimpact of the water soluble Q-dots on macrophage cells compared toindividual components. Positive control includes only growth media.Negative control has deionized water instead of growth media to signifycell death.

FIG. 23 shows cytotoxicity assay using Alamar Blue, showing the toxicimpact of the water soluble Q-dots on macrophage cells compared toindividual components. Positive control includes only growth media (FIG.A). Negative control (FIG. B) has deionized water instead of growthmedia to signify cell death. Bare Q-dots incubated with macrophage cells(FIG. C), NAC Q-dots incubated with macrophage cells (FIG. D), andsodium gluconate coated Q-dots incubated with macrophage cells (FIG. E)all showing negative cytotoxic effects as there are many cells preparingfor cell division. FIG. F, shows the toxic impact of just Zn acetatealone where many cells have lost their projections and cell fragmentsare present in the surrounding media.

DETAILED DESCRIPTION OF THE NON-LIMITING EMBODIMENTS I. GeneralConsiderations

Embodiments provide a light-sensitive particle with enhanced purity andperformance, and a method for preparing the light-sensitive particlewith the enhanced purity and the enhanced performance. To achieve theforegoing results, the embodiments utilize when fabricating alight-sensitive particle in accordance with the embodiments an aqueoussolution method that uses at least one water soluble metal precursormaterial and at least one water soluble dopant precursor material. Themethod comprises a sol-gel method that may be undertaken at roomtemperature while using water soluble and residue free source materials,along with an optional acid material or an optional base material as alight-selective particulate precipitant material.

While the embodiments illustrate as a light-sensitive particle alight-emitting particle such as a fluorescent light-emitting particlefurther such as a Q-dot fluorescent light-emitting particle, theembodiments are not intended to be so limited. Rather the embodimentsare intended to include light-sensitive particles including but notlimited to light-emitting particles and light-absorbing particles. Suchlight absorbing particles may include but are not necessarily limited tophotovoltaic particles.

Within the context of the embodiments, a metal precursor material maycomprise a water soluble metal material selected from the groupincluding but not limited to salts (i.e., and in particular acetatesalts) of metals including but not limited to metals of atomic numbers25 to 30 and additionally up to 48. More specific and more preferredwithin the embodiments metals include manganese, zinc and cadmium asacetate salts. Acetate salts are particularly desirable within thecontext of the embodiments insofar as acetate residues are oftenthermally decomposable and may be residue free.

Other particular embodiments are not strictly limited to metal-donormaterial based light emitting material, but are also intended to includeother light-emitting materials such as but not limited to light emittingsemiconductor materials which are described further below and which aregenerally compound complementary semiconductor materials.

Within the context of the embodiments, a dopant precursor material maybe selected from the group including but not limited to sodium sulfidedopant precursor materials and sodium selenide dopant precursormaterials. Other dopant precursor materials are not excluded whichinclude but are not limited to elements of the lanthanide region of theperiodic table such as but not limited to dysprosium and gadolinium.

The sol-gel preparation method that may be used to form thelight-sensitive particles in accordance with the embodiments maygenerally be undertaken at a temperature from about 20 to about 37degrees centigrade for a preparation (i.e., synthesis) time period fromabout 5 to about 10 minutes, although greater or lesser preparationtimes and preparation temperatures are not excluded.

In general, the embodiments provide a sol-gel method for preparing alight sensitive particle absent the use of a surfactant, thus providingthe light sensitive particle absent a surfactant residue. Within theembodiments the light sensitive particle may comprise a simple lightsensitive particle having a homogeneous composition. The resultinglight-sensitive particle may also be a core-shell particle having afirst composition for the core and a second composition different thanthe first composition for the shell that surrounds the core. Moreover,the embodiments also include a sol-gel method for preparing a core-shellcomposite nanoparticle that includes at least one light-sensitivecomponent (i.e., one of the core component and the shell component) andat least one insulator component which may be a transparent insulatorcomponent. This latter group of composite light-sensitive particles mayinclude the insulator layer as either a core layer or a shell layer. Thepresence of the insulator layer within the composite light-sensitiveparticle provides the light-sensitive particle with either desirableoptical properties such as photo-stability and resistance tophoto-bleaching or alternatively desirable surface properties such asstable water dispersability, longer shelf-life and specified targetingfor biomedical and agricultural applications.

II. Specific Considerations

Embodiments of the present disclosure provide in-part for methods ofpreparing fluorescent gel particles, and the like, while using a sol-gelmethod. In an embodiment, fluorescent light-emitting gel particles ofthe present disclosure are 100% free of surfactant, as compared to knowncompositions made using surfactants, where removal of all the surfactantpost light emitting gel particle preparation can be very difficult. Inan embodiment, the method is a water based one-pot chemical synthesismethod that is rapid and relies on simple mixing steps. This method andthe fluorescent light-emitting gel particles that result from the methodare of particular interest to electronic, optoelectronic and agricultureindustries.

Embodiments of the present disclosure can include mixing a first metalprecursor material (e.g., metal compound such as cadmium acetate, zincacetate, manganese acetate, or the like) with a first dopant precursormaterial (e.g., sodium sulfide or the like) to form a first metal-dopantmaterial. Next the pH of the composition is adjusted to about 3 to 6 toform the light-emitting fluorescent gel particles. The process offorming the fluorescent gel particles is surfactant free (e.g., does notinclude surfactants used to form Q-dot particles and the like), which isdistinct with other processes. In an embodiment, the first metalprecursor material, the first dopant precursor material, the secondmetal precursor material and the second dopant precursor material are inthe aqueous phase. In an embodiment, the fluorescent light-emitting gelparticles can be selected from: CdS:Mn/ZnS, ZnS:Mn, MnS;ZnS, or thelike. In an embodiment, the formed fluorescent light-emitting gelparticles are 100% free of surfactant. Additional details are providedin the experimental examples.

The present disclosure describes a surfactant-free method of preparingmetal/dopant based water-dispersible fluorescent light-emitting gelparticles (such as CdS:Mn/ZnS, ZnS:Mn and MnS;/ZnS) particles (analogousterminology is fluorescent quantum dots, Q-dot particles). This is aone-pot water based chemical synthesis method that is simple enough toproduce high-quality gel particles in scalable quantity (metric tonscale). The process is rapid and relies upon simple mixing steps.Surfactant-free fluorescent light-emitting gel particles areparticularly desirable for applications in electronic optoelectronic andagriculture industries.

Traditionally fluorescent light-emitting Q-dot particles includingmetal/dopant based Q-dot particles are synthesized by a wet chemicalmethod that is not a sol-gel method. In all cases, a mixture of asurfactant and a capping agent (such as a mixture of trioctyl phosphine(TOP; a surfactant) and trioctylphosphine oxide (TOPO; a capping agent),commonly known as TOP/TOPO mixture) is used. Water-in-oil (W/O)microemulsion method is also used to prepare (i.e., synthesize) fairlyhigh-quality metal/dopant based Q-dot particles at room temperature.However, a surfactant is used to prepare a W/O micro-emulsion. Aconventional Q-dot particle purification process is extremelycumbersome, expensive and generates undesirable waste. Moreover,complete removal of a surfactant residue from a Q-dot particle surfaceis extremely challenging without compromising electronic andoptoelectronic properties of the Q-dot. Due to these limitations, bulkscale production of high-quality metal/dopant based Q-dot particles hasnot been possible.

Water dispersability of the disclosed fluorescent light-emitting gelparticles may be achieved through surface modifications with hydrophiliccoating agents which include, but are not necessarily limited to sodiumgluconate, sodium salicylate, N-acetylcysteine (antioxidant molecule),glutathione (antioxidant tripeptide molecule), quaternary ammonium saltsand tetraethylorthosilicate materials. Other materials that may be usedare listed in the foregoing descriptions of the drawings. Suchfluorescent light-emitting gel particle modification does not compromisethe integrity of the metal/dopant core of the fluorescent light-emittinggel particles. Fluorescent light-emitting gel particles size andcrystallinity may be characterized using HRTEM in a dry state. Theaverage fluorescent light-emitting gel particle crystal size was about 5nm. A fluorescent light-emitting gel particle with a hydrophilic coatingis characterized in solution using dynamic light scattering (DLS)technique. DLS measured the hydrodynamic diameter of the fluorescentlight emitting gel particles in the range of about 18-20 nm,respectively, and show crystal sizes ranging from about 5-10 nm withouthydrophilic coating and about 18-20 nm with hydrophilic coating.

Fourier-transform infrared (FTIR) spectroscopy measurements oflyophilized samples confirmed the presence of hydrophilic coating on thefluorescent light-emitting gel particles when compared to barefluorescent light-emitting gel particles. These fluorescentlight-emitting gel particles emit at ˜587 nm with 326 nm excitation(ZnS:Mn) and 590 nm with 350 nm excitation (CdS:Mn/ZnS). A preparationprotocol and fluorescent sol particles characterization data arepresented below.

In addition to the fluorescent gel particles described above and below,embodiments of the present disclosure can be directed to fluorescentlight-emitting gel particles having other chemical compositions. As aresult, the first metal core precursor material, the first dopant coreprecursor material, the second metal shell precursor material and thesecond dopant shell precursor material are or may be independentlyselected to form the desired fluorescent light-emitting gel particles.

As mentioned above, nano-particles in accordance with the disclosure andthe embodiments may include, but are not necessarily limited to,fluorescent light emitting semiconductor Q-dot particles. In general,Q-dot particles include a core material and a capping (also called ashell) material. The “core” is a semiconductor or doped or undopedinsulator nano-particle with dimensions of about 1 to 250 nm. While anycore of the IIB-VIA, IIIA-VA, or IVA-IVA, IVA-VIA, IB-IIIA-VIAsemiconductors or doped or undoped insulator can be used in the contextof the present disclosure, the core may or may not be a luminescent NP,whose luminance may be increased by a capping layer whereby the cappinglayer provides further surface passivation and protection to the corefor the fluorescence process. Recombination of the electron-hole pairbecomes possible as opposed to without the capping layer where theelectron-hole recombination event would not take place. A IIB-VIAsemiconductor is a compound that contains at least one element fromGroup IIB and at least one element from Group VIA of the periodic table,and so on. The core can include two or more elements. In an embodiment,the core of the nanoparticles can also be a transition metal oxide orlanthanide metal oxide NP doped with rare earth or transition metalions, or a combination thereof. In another embodiment, the core of theNP is a Group IA or IIA or solid solutions between Group IA elements,Group IIA elements, and combination thereof, or lanthanide metals boundto a Group VIIA halide with or without a dopant, particularly rare earthions and transition metal ions, Ce-doped Lu, Y and Gd oxyorthosilicates,Ce-doped oxyorthosilicates made with a combination of at least two ofthe elements Y, Lu and Gd, Ce-doped Sr or Ba hafanate, or alloys such asLu_(2x)Gd_(2(1-x))SiO₅:Ce or Ce_(x)La_(1-x)F₃ (x is variable from aboutone to zero). In one embodiment, the core is an IIB-VIA, IIIA-VA, orIVA-IVA semiconductor that can be about 1 nm to 40 nm, about 1 nm to 30nm, about 1 nm to 20 nm, or about 1 nm to 10 nm in diameter. In anotherembodiment, the core can be an IIB-VIA semiconductor and can be about 2nm to 10 nm in diameter. For example, the core can be CdS, CdSe, CdTe,ZnSe, ZnS, ZnS:Ag, ZnO:Ag, PbS, PbSe, or an alloy such asCd_(x)Zn_(1-x)Se_(y)Te_(1-y), where x is a variable from one to zero andy is variable from about one to zero. In an embodiment the core is CdTe.

The “cap” or “shell” may be a semiconductor or insulator that differsfrom or is the same as the semiconductor or insulator of the core andbinds to the core, thereby forming a surface layer on the core. A shellcan differ from the core and/or other shells by means of its chemicalcomposition, and/or the presence of one or more dopants, and/ordifferent amounts of a given dopant. The shell typically passivates thecore by having a higher band gap than the core, and having an energyoffset in the top of the valence band and bottom of the conduction bandsuch that electrons and/or holes may be confined to the core by theshell. Each shell encloses, partially (e.g., about 50% or more, about60% or more, about 70% or more, about 80% or more, about 90% or more,about 95% or more, about 99% or more) or totally, the adjacent shellcloser to the core. In one embodiment, the shell can be a IIB-VIAsemiconductor of high band gap. For example, the shell can be ZnS or CdSon a core of CdSe_(y)Te_(1-y) (y is variable from about one to zero).Other combinations of the core and shell can include, but are notlimited to, the shell is ZnS when the core is CdSe or CdS, and the shellis CdS when the core is CdSe. In an embodiment, the shell may also be anorganic film, such as silicones, thiophenes, trioctylphosphine,trioctylphosphine oxide, or a combination thereof. Other exemplary NP'sinclude, but are not limited to, CdS, ZnSe, ZnS:Ag, ZnS:Cu, ZnO, CdSe,CdTe, CdSe_(x)Te_(1-x) (x is variable from about one to zero), InAs,InP, PbTe, PbSe, PbS, HgS, HgSe, HgTe, CdHgTe, and GaAs. The thicknessof the shell can be about 0.1 to 20 nm, about 0.1 to 5 nm, or about 0.1to 2 nm covering the core.

III. Experimental Measurements

FIG. 1A (left) shows room lighting images illustrating surfactant freegel particles on the left and micro-emulsion synthesized glow particleson the right. FIG. 1B (right) shows UV-excitation image showing thefluorescence of surfactant free gel particles on the |oft andmicro-emulsion synthesized gel particles on the right

FIG. 2A shows high resolution transmission electron microscopy (HRTEM)images showing 5 nm sized gel particles. Selective area electrondiffraction (SAED) shows the crystallinity and lattice plane spacings.FIG. 2B shows electron dispersion x-ray (EDX) spectroscopy confirmingthe particle composition of ZnS:Mn gel particles on a carbon coatedcopper grid.

FIG. 3A and FIG. 3B shows fluorescence emission of CdS:Mn/ZnS andZnS:Mn/ZnS gel particles measured using a NanoLog spectrofluorimeter(SPEX, Jobin Yvon Horiba) without a neutral density filter. Spectra werecollected for washed gel particles that were removed from amicroemulsion and redispersed in water.

FIG. 4A and FIG. 4B show fluorescence activation of CdS:Mn/ZnSsemiconductor and increasing intensity with decreasing pH. Fluorescenceintensity was measured using the NanoLog spectrofluorimeter (SPEX, JobinYvon Horiba) with a neutral density filter.

FIG. 5A and FIG. 5B show fluorescence activation of ZnS:Mn semiconductorand increasing intensity with decreasing pH. Fluorescence intensity wasmeasured using the NanoLog spectrofluorimeter (SPEX, Jobin Yvon Horiba)with a neutral density filter.

FIG. 6A and FIG. 6B show fluorescence quenching of ZnS:Mn semiconductorwith increasing H₂0₂ concentration showing a stow oxidation of ZnSsemiconductor to ZnO. Fluorescence intensity was measured using theNanoLog spectrofluorimeter (SPEX, Jobin Yvon Horiba). A neutral densityfilter was used only to measure the initial gel particle fluorescencebefore hydrogen peroxide addition.

FIG. 7A and FIG. 7B show fluorescence quenching of ZnS:Mn semiconductorwith increasing Quat surfactant volume showing the slow coating ofZnS:Mn semiconductor to ZnS:Mn/Quat. A neutral density filter was usedonly to measure the initial gel particle fluorescence before Quataddition.

FIG. 8 shows 200 ml large scale synthesis of surface modified surfactantfree gel particles showing long term shelf life and water solubility.Sodium salicylate (SS), TEOS (TE), and sodium gluconate (SG) wereincorporated as solubilizing agents.

FIG. 9 Shows UV-visible absorbance of CdS:Mn/ZnS gel particle coatedwith TEOS (silica), sodium salicylate and sodium gluconate was collectedusing a Cary 300 UV-visible spectrophotometer. Respective controls areincluded for comparison. Bare sol-gel particles were dilutedappropriately in order to obtain an absorbance of 0.1 at 350 nm. Coatingagents improve gel particle solubility as noted by the reduced lightdiffraction between bare and coated gel particles.

FIG. 10 shows fluorescence emission of CdS:Mn/ZnS semiconductor showingthe maturation of the sol-gel particle and Mn²⁺ dopant environment asfluorescence increased between Day 1-Day 6. In addition, relativefluorescence emissions for sodium gluconate, sodium salicylate, and TEOScoated gel particles.

FIG. 11 shows fluorescence emission of ZnS:Mn semiconductor showing thematuration of the gel particle and Mn²⁺ dopant environment asfluorescence increased between Day 1-Day 6.

FIG. 12 shows FTIR spectra of base and coated fluorescent emitter gelparticles.

FIG. 13 shows ambient light image of water soluble ZnS:Mn gelnanoparticles (FIG. A) showing (from left to right) glutathion (GSH)coated, N-acetyl cysteine (NAC) coated, sodium gluconate (SG) coated,NAC/GSH co-coated, NAC-fluoresceine isothiocyanate (FllC) coated, andbare uncoated. Same samples showing fluorescence emission under 254 nmexcitation (FIG. B) and 365 nm excitation (FIG. C).

FIG. 14 shows UV visible absorbance spectra of water soluble ZnS gelQ-dots at 326 nm excitation. ZnS bare (blue) at pH 1. ZnS NAC (red,N-acetyl cysteine) at pH 9.26, ZnS SG at pH 5.6 (green, sodiumgluconate), ZnS NAC-FITC at pH 9 (purple, fluoresceine isothiocyanate),ZnS NAC/GSH (light blue, co-coated with NAC and glutathione), and ZnSGSH pH 8 (orange) have all been standardized to 0.1 absorbance at 326 nmusing a CaryWin UV Spectrophotometer. Peak absorbance at 490 nmindicates the presence of FITC on the ZNS NAC-FITC Q-dot. At 200 nm theZnS SG absorbs about 0.85 and the ZnS bare absorbs about 0.38. Theremainder of the ZnS compositions provide extinction of light at about300 nm

FIG. 15 shows peak fluorescence emission of water soluble ZnS gel Q-dotsat 326 nm excitation. ZnS Bare (Blue) at pH 1. ZnS NAC (red,N-acetylcysteine) at pH 9.26, ZnS SG at pH 5.6 (green, sodium gluconateZnS NAC-FITC at pH 9 (purple, fluoresceine isothiocyanate ZnS NAC/GSH(black, co-coated with NAC and glutathione ZnS GSH pH 8 (orange), and MENAC pH 5.6 (dark blue, ZnS Q-dots prepared in w/o microemulsion) haveall been standardized to 0.1 absorbance at 326 nm using a CaryWin UVSpectrophotometer. ME NAC included as a comparison example. In order ofdecreasing absorbance at 600 nm is bare, GSH, NAC, NAC-GSH, AC-FITC SGand ME-NAC

FIG. 16 shows fluorescence emission of ZnS NAC-FITC (N-acetyl cysteinelinked fluoresceine isothiocyanate) with 400 nm excitation showing the510 nm emission of FITC confirming the presence of an organic dye on theQ-dot and thus providing a light sensitive particle that includes ametal dopant inorganic semiconductor light sensitive component and anorganic fluorescent dye light sensitive component.

FIG. 17 shows dynamic light scattering (DLS) of bare ZnS Q-dotsdispersed in water at neutral pH showing micron-sized particles. AverageZeta potential is 10.77 mV

FIG. 18 shows dynamic light scattering (DLS) of coated ZnS NAC Q-dotssolubilized in water at pH 9.26 showing an average particle size of35.28 nm. Average Zeta potential was −15.87 mV.

FIG. 19 shows dynamic light scattering (DLS) of coated ZnS sodiumgluconate Q-dots solubilized in water at pH 5.6 showing an averageparticle size of 1407 nm. Average Zeta potential was −30.13

FIG. 20 shows dynamic Light Scattering (DLS) of coated ZnS NAC/GSHQ-dots solubilized in water at pH 9.26 showing average particle sizesranging from 8.6 nm to 104 nm.

FIG. 21 shows dynamic light scattering (DLS) of coated ZnS GSH Q-dotssolubilized in water at pH 8 showing an average particle size of 60.80nm.

FIG. 22 shows cytotoxicity assay using Alamar Blue, showing the toxicimpact of the water soluble Q-dots on macrophage cells compared toindividual components. Positive control includes only growth media.Negative control has deionized water instead of growth media to signifycell death.

FIG. 23 shows cytotoxicity assay using Alamar Blue, showing the toxicimpact of the water soluble Q-dots on macrophage cells compared toindividual components. Positive control includes only growth media (FIG.A). Negative control (FIG. B) has deionized water instead of growthmedia to signify cell death. Bare Q-dots incubated with macrophage cells(FIG. C), NAC Q-dots incubated with macrophage cells (FIG. D), andsodium gluconate coated Q-dots incubated with macrophage cells (FIG. E)all showing negative cytotoxic effects as there are many cells preparingfor cell division. FIG. F, shows the toxic impact of just Zn acetatealone where many cells have lost their projections and cell fragmentsare present in the surrounding media.

IV. Particulate Preparation

Table I shows a comparison of various characteristics for Q-dotparticles produced using conventional methods, and in accordance withthe embodiments.

TABLE I Comparison of Methods for Fluorescent Particle Preparation Qdotsynthesis CdS:Ma/ZaS or CuInS/ZnS (Hot-phase parameters and opticalZaS:Ma/ZnS (W/O CdSe (Hot Phase synthesis; another propertiesMicroemulsion) synthesis) example - alloy core based) Sol-GlowTemperature Room Temperature High Temperature High Temperature Roomconditions (>150 degree C.) (>150 degree C.) Temperature Inert synthesisNo Yes Yes Not required conditions required? Use of surfactant? Yes YesYes Surfactant free Use of mixed solvents? Yes Yes Yes No (water-based)Time Sensitive? Yes Yes Yes No Time Consuming? Yes Yes Yes No (tedious)Use of non-aqueous Yes Yes Yes No solvents? Further surface Yes Yes YesYes modification (for bioconjugation, improving solubility etc)possible? High quality crystals? Yes Yes Yes Yes Size-tunable emissionLimited (dopant Yes Yes Limited (dopant property? based emission) basedemission) Photostable? Yes Yes Yes Yes Fluorescently bright? Yes Yes YesYes

V. Specific Preparation Methods for Q-Dot Particles 1. Water-in-Oil(W/O) Micro-emulsion Preparation of CdS:Mn/ZnS and ZnS:Mn/ZnS Q-dots

-   -   A. Supplies        -   3 conical flasks (regular washed, acid washed, base washed,            rinsed, dried.)        -   3 magnetic stir bars (clean)        -   3 glass vials w/ caps        -   burette        -   cadmium acetate dihydrate (MW 266.52)        -   zinc acetate dehydrate 99.999+% (MW 219.5 g)        -   manganese acetate tetrahydrate (MW 245.09 g)        -   sodium sulfide (MW 78.04)        -   dioctyl sulfosuccinate sodium salt [AOT] (MW 444.55 g)        -   heptane (MW 100.21 g)        -   deionized water    -   B. Solvent Ratios        -   AOT:heptane—0.0892        -   water:heptane—0.036    -   C. Stock Preparation        -   Stock Solution 1            -   266 mg cadmium acetate dihydrate (0.1 mol) or 219 mg                zinc acetate dihydrate for ZnS:Mn/ZnS synthesis            -   4.9 mg manganese acetate or 3.9 mg for ZnS:Mn/ZnS (1.8%                of core metal mass)            -   mix in 10 ml DI water in glass vial until dissolved        -   Stock solution 2            -   257.5 mg sodium sulfide (0.66 mol)            -   mix in 5 ml DI water in glass vial until dissolved        -   Stock solution 3            -   285.25 mg zinc acetate dihydrate (0.26 mol)            -   mix in 5 ml DI water in glass vial until dissolved        -   Flask A            -   25 ml heptane            -   2.23 g AOT            -   mix in conical flask with magnetic stir bar until AOT is                dissolved (˜15 min) and cover from light with aluminum                foil        -   Flask B            -   75 ml heptane            -   6.69 g AOT            -   mix in conical flask with magnetic stir bar until AOT is                dissolved (˜15 min) and cover from light with aluminum                foil        -   Flask C            -   75 ml heptane            -   6.69 g AOT            -   mix in conical flask with magnetic stir bar until AOT is                dissolved (˜15 min) and cover from light with aluminum                foil    -   D. Synthesis (briefly sonicate all stock solutions prior to        mixing with the AOT/Heptane mixture)        -   add 2.7 ml of stock solution 2 into Flask B and stir for 1            hour (wait 30 min and then move to step 2)        -   add 0.9 ml of stock solution 1 into Flask A and stir for 30            min (wait 15 min and then move to step 3)        -   both solutions should finish stirring at the same time        -   add 2.7 ml of stock solution 3 into Flask C dropwise and let            stir for 30 min. when Flask A and B have finished mixing,            pour Flask A into Flask B (a yellow color change will occur            for CdS:Mn/ZnS Q-dot) and mix for 15 min (Flask A+B)        -   all solutions must finish mixing at the same time        -   using the burette, add Flask C to mixed Flask A+B at a rate            of 1-2 ml/min (very important)        -   observe fluorescence using a handheld UV light source and            securely cover with foil for 24 hours        -   color should be a bright yellow to yellow-orange color.    -   E. Washing        -   Transfer desired volume of quantum dot (Q-dot)            micro-emulsion (ME) into centrifuge tube and add twice that            volume containing acetone/ethanol mixture (1:1 v/v)            Centrifuge at 11,000 rpm for 10 min and remove            nonfluorescent supernatant.        -   Disperse fluorescent pellet in acetone (equal volume to            withdrawn Q-dot ME) via vortexing and sonication.        -   Repeat steps 2 and 3 three times        -   Disperse fluorescent pellet in heptane and repeat step 2        -   Repeat step 5 and 2        -   Disperse fluorescent pellet in Acetone and repeat step 2        -   Decant acetone and evaporate excess acetone using a hot            water bath.        -   Disperse washed particles in water (Note—˜80% of the            surfactant will be removed)

2. Sol-Gel Preparation of CdS:Mn/ZnS and ZnS:Mn in Accordance WithEmbodiments

-   -   A. Supplies        -   glass vials w/ caps        -   cadmium acetate dihydrate (MW 266.52)        -   zinc acetate dehydrate 99.999+% (MW 219.5 g)        -   manganese acetate tetrahydrate (MW 245.09 g)        -   sodium sulfide (MW 78.04)        -   6N hydrochloric acid        -   6N NaOH (Optional)        -   deionized water

B. Stock Preparation

-   -   Stock Solution 1        -   266 mg cadmium acetate dihydrate (0.1 mol) or 219 mg zinc            acetate dihydrate for ZnS:Mn/ZnS synthesis        -   4.9 mg manganese acetate or 3.9 mg for ZnS:Mn/ZnS (1.8% of            core metal mass) mix in 10 ml DI water in glass vial until            dissolved    -   Stock solution 2        -   257.5 mg sodium sulfide (0.66 mol)        -   mix in 5 ml DI water in glass vial until dissolved    -   Stock solution 3        -   285.25 mg zinc acetate dihydrate (0.26 mol)        -   mix in 5 ml DI water in glass vial until dissolved    -   C. Preparation (briefly sonicate all stock solutions prior to        combination)        -   using a glass container (beaker, flask, vial) combine 2.7 ml            of stock solution 3 and        -   0.9 ml of stock solution 1 and briefly mix        -   add 2.7 ml of stock solution 2 dropwise while mixing        -   lower the pH to between 6-3 by adding 200-400 μL of 6N HCl            dropwise (optimal fluorescence is achieved at lower pH)        -   (optional) if necessary, adjusting pH to neutral after            achieving optimal fluorescence can be done using 6N NaOH    -   D. Purification—for further modification/use, particles can be        washed to remove excess salt centrifuge at 11,000 rpm for 5 min,        decant nonfluorescent supernatant, disperse in deionized water

3. CdSe Q-dot Hot Phase Preparation

-   -   1. Reference: Evan R. Trivedi and Shelby L. Hatch. “Synthesis        and Size Dependent Properties of CdSe Quantum Dots,” Department        of Chemistry, Northwestern University, n.d. Web. 12 May 2013.    -   2. Preparation Sequence        -   a. Prepare Se stock solution by dissolving Se beads in            1-octadecene with trioctylphosphine. It takes-3 hrs at high            temperature for the Se beads to dissolve        -   b. To a 25 mL round-bottom flask, add a magnetic stir bar            and 13 mg CdO (CdO should be prepackaged in 13 mg portions).        -   b. Add 0.6 mL oleic acid and 10 mL 1-octadecene to the            round-bottom.        -   c. Clamp the round-bottom flask into the metal heating            mantle on the hot plate. Place a thermometer into the            heating mantle. Do not allow the thermometer to heat up            beyond the maximum temperature reading (˜250° C.)        -   d. Turn on the heat and magnetic stirring.        -   e. When the Se stock solution is added, aliquots must be            removed every 30 seconds.        -   f. Monitor the reaction mixture carefully and add 1 mL Se            stock solution when all of the CdO has dissolved (solution            should be clear to pale yellow).        -   g. Remove aliquots (˜1 mL) every 30 seconds with the glass            pipets.        -   h. Continue collection for about three minutes or until the            solution no longer changes color.        -   i. Turn off heat and remove the round-bottom flask from the            heating mantle. If the flask is allowed to cool while on the            heating mantle, it will break.        -   j. Irradiate the quantum dot solutions with UV light and            make observations.

4. Hot Phase CuInS/ZnS Q-dot Synthesis

Reference: Woo-Seuk Song and Heesun Yang, Efficient White-Light-EmittingDiodes Fabricated from Highly Fluorescent Copper Indium SulfideCore/Shell Quantum Dots. Chemistry of Materials 2012 24 (10), 1961-1967

-   -   Materials <Aldrich Product number>        -   1. Cu iodide: 215554        -   2. In acetate: 510270        -   3. DDT: 471364        -   4. ODE: O806        -   5. Zn stearate: 26423        -   6. Three neck flask        -   7. Hot plate        -   8. Syringes        -   9. Argon Gas    -   Preparation        -   CIS (Cu:In=1:4) core Q-dots        -   1. Cu iodide→0.125 mmol (0.024 g)        -   2. In acetate→0.5 mmol (0.146 g)        -   3. DDT→5 mL    -   Loading in 50 mL of three neck flask        -   Preparation of ZnS shell solution        -   1. Zn stearate 4 mmol (2.528 g)        -   2. 1-octadecene 4 mL        -   3. DDT 1 mL        -   4. Heat on hot plate at 190° C., then use it as shell            solution    -   Synthesis    -   1. Heat contents in 50 mL flask at 100° C. for 30 min    -   2. Quickly Heat to 230° C. within 10 min under a purge with Ar        atmosphere and keep at that temperature for 5 min    -   3. Add ZnS shell dropwise    -   4. Heat to 240° C. and maintain for 60-70 min    -   5. Cool to RT and wash with ethanol/chloroform solvent (1:1 v/v)    -   6. Disperse in chloroform        5. Capped Q-dot Synthesis protocol (Low Temperature Aqueous        Synthesis) Sun, Q.; Fu, S.; Dong, T.; Liu, S.; Huang, C.,        Aqueous Synthesis and Characterization of TGA-capped CdSe        Quantum Dots at Freezing Temperature. Molecules 2012, 17,        8430-8438.        1. Add 0.05 mmol Se powder and 0.15 mmol NaBH4 and 3.0 mL        deionized water to a 25 mL round-bottom flask, and keep at 0° C.        (ice bath) for 30 min to give a mixture A.        2. Mix 8.75 mL 0.2 mol/L CdCl2 and 1.1 mmol TGA in a        round-bottom flask (II), and adjust the pH to 10.50 with 1 mol/L        NaOH, followed by addition of mixture A via syringe at 0° C.        under a nitrogen atmosphere. (solution color becomes bright        yellow)        To obtain TGA-capped CdSe QDs, acetone precipitation with        centrifugation at 12,000 rpm for 15 min. Treat with acetone for        three repeated cycles to remove the contaminants

It should be noted that ratios, concentrations, amounts, and othernumerical data may be expressed herein in a range format. It is to beunderstood that such a range format is used for convenience and brevity,and thus, should be interpreted in a flexible manner to include not onlythe numerical values explicitly recited as the limits of the range, butalso to include all the individual numerical values or sub-rangesencompassed within that range as if each numerical value and sub-rangeis explicitly recited. To illustrate, a concentration range of “about0.1% to about 5%” should be interpreted to include not only theexplicitly recited concentration of about 0.1 wt % to about 5 wt %, butalso include individual concentrations (e.g., 1%, 2%, 3%, and 4%) andthe sub-ranges (e.g., 0.5%, 1.1%, 2.2%, 3.3%, and 4.4%) within theindicated range. In an embodiment, the term “about” can includetraditional rounding according to the measuring technique and thenumerical value. In addition, the phrase “about ‘x’ to ‘y’” includes“about ‘x’ to about ‘y’”.

While only a few embodiments of the present disclosure have been shownand described herein, it will become apparent to those skilled in theart that various modifications and changes can be made in the presentdisclosure without departing from the spirit and scope of the presentdisclosure. All such modification and changes coming within the scope ofthe appended claims are intended to be carried out thereby.

This disclosure is not limited to particular embodiments described, andas such may, of course, vary. The terminology used herein serves thepurpose of describing particular embodiments only, and is not intendedto be limiting, since the scope of the present disclosure will belimited only by the appended claims.

Where a range of values is provided, each intervening value, to thetenth of the unit of the lower limit unless the context clearly dictatesotherwise, between the upper and lower limit of that range and any otherstated or intervening value in that stated range, is encompassed withinthe disclosure. The upper and lower limits of these smaller ranges mayindependently be included in the smaller ranges and are also encompassedwithin the disclosure, subject to any specifically excluded limit in thestated range. Where the stated range includes one or both of the limits,ranges excluding either or both of those included limits are alsoincluded in the disclosure.

Embodiments of the present disclosure will employ, unless otherwiseindicated, techniques of material science, chemistry, and the like,which are within the skill of the art. Such techniques are explainedfully in the literature.

The following examples are put forth so as to provide those of ordinaryskill in the art with a complete disclosure and description of how toperform the methods and use the compositions and compounds disclosed andclaimed herein. Efforts have been made to ensure accuracy with respectto numbers (e.g., amounts, temperature, etc.), but some errors anddeviations should be accounted for. Unless indicated otherwise, partsare parts by weight, temperature is in ° C., and pressure is at or nearatmospheric. Standard temperature and pressure are defined as 20° C. and1 atmosphere.

Before the embodiments of the present disclosure are described indetail, it is to be understood that, unless otherwise indicated, thepresent disclosure is not limited to particular materials, reagents,reaction materials, manufacturing processes, dimensions, frequencyranges, applications, or the like, as such can vary. It is also to beunderstood that the terminology used herein is for purposes ofdescribing particular embodiments only, and is not intended to belimiting. It is also possible in the present disclosure that steps canbe executed in different sequence, where this is logically possible. Itis also possible that the embodiments of the present disclosure can beapplied to additional embodiments involving measurements beyond theexamples described herein, which are not intended to be limiting. It isfurthermore possible that the embodiments of the present disclosure canbe combined or integrated with other measurement techniques beyond theexamples described herein, which are not intended to be limiting.

It should be noted that, as used in the specification and the appendedclaims, the singular forms “a,” “an,” and “the” include plural referentsunless the context clearly dictates otherwise. Thus, for example,reference to “a support” includes a plurality of supports. In thisspecification and in the claims that follow, reference will be made to anumber of terms that shall be defined to have the following meaningsunless a contrary intention is apparent.

All references, including publications, patent applications, and patentscited herein are hereby incorporated by reference in their entireties tothe extent allowed, and as if each reference was individually andspecifically indicated to be incorporated by reference and was set forthin its entirety herein.

The use of the terms “a” and “an” and “the” and similar referents in thecontext of describing the invention (especially in the context of thefollowing claims) is to be construed to cover both the singular and theplural, unless otherwise indicated herein or clearly contradicted bycontext. The terms “comprising,” “having,” “including,” and “containing”are to be construed as open-ended terms (i.e., meaning “including, butnot limited to,”) unless otherwise noted. The term “connected” is to beconstrued as partly or wholly contained within, attached to, or joinedtogether, even if there is something intervening.

The recitation of ranges of values herein is merely intended to serve asa shorthand method of referring individually to each separate valuefalling within the range, unless otherwise indicated herein, and eachseparate value is incorporated into the specification as if it wasindividually recited herein.

All methods described herein may be performed in any suitable orderunless otherwise indicated herein or otherwise clearly contradicted bycontext. The use of any and all examples, or exemplary language (e.g.,“such as”) provided herein, is intended merely to better illuminateembodiments of the invention and does not impose a limitation on thescope of the invention unless otherwise claimed.

No language in the specification should be construed as indicating anynon-claimed element as essential to the practice of the invention.

It will be apparent to those skilled in the art that variousmodifications and variations can be made to the present inventionwithout departing from the spirit and scope of the invention. There isno intention to limit the invention to the specific form or formsdisclosed, but on the contrary, the intention is to cover allmodifications, alternative constructions, and equivalents falling withinthe spirit and scope of the invention, as defined in the appendedclaims. Thus, it is intended that the present invention cover themodifications and variations of this invention provided they come withinthe scope of the appended claims and their equivalents.

What is claimed is:
 1. A particle comprising at least one portion thatincludes a light-selective composition absent a surfactant residue. 2.The particle of claim 1 wherein the particle has a diameter from about 5to about 10 nanometers.
 3. The particle of claim 2 wherein thelight-selective composition comprises a light-emitting composition. 4.The particle of claim 3 wherein the light emitting composition comprisesa fluorescent light-emitting composition.
 5. The particle of claim 4wherein the fluorescent light-emitting composition comprises a quantumdot.
 6. The particle of claim 1 wherein the particle comprises acore-shell particle.
 7. The particle of claim 6 wherein at least a corelayer within the core-shell particle comprises the light-selectivematerial.
 8. The particle of claim 6 wherein at least a shell layerwithin the core-shell particle comprises the light selective material.9. The particle of claim 6 wherein each of a core layer and a shelllayer within the core-shell particle comprise a light selectivematerial.
 10. The particle of claim 6 wherein one of the core layer andthe shell layer within the core-shell particle comprises an insulatormaterial formed from a precursor material selected from the groupconsisting of sodium gluconate, sodium salicylate, N-acetylcysteine andglutathione.
 11. The particle of claim 6 wherein the shell layer withinthe core-shell particle comprises an insulator material.
 12. A methodfor preparing a particle comprising: mixing in an aqueous solutionabsent a surfactant material at least one metal precursor material andat least one dopant precursor material to provide a metal-dopantmaterial particle absent a surfactant residue.
 13. The method of claim12 further comprising after mixing in the aqueous solution absent thesurfactant material the at least one metal precursor material and the atleast one dopant precursor material adjusting a pH of the aqueoussolution to facilitate production of the metal-dopant particle absentthe surfactant residue.
 14. The method of claim 13 wherein the pH isadjusted to about 3 to about
 6. 15. The method of claim 12 wherein themetal-dopant material particle comprises a binary semiconductormaterial.
 16. A method for preparing a particle comprising: mixing in anaqueous solution absent a surfactant material at least one metalprecursor material and at least one dopant precursor material to providea metal-dopant material particle absent a surfactant residue; andfurther reacting the metal-dopant material particle absent thesurfactant residue with an encapsulant precursor material to provide acore-shell encapsulated metal—dopant material particle.
 17. The methodof claim 16 wherein the encapsulated metal-dopant material particle isencapsulated with an insulator material.
 18. The method of claim 16wherein the encapsulant precursor material comprises sodium gluconate.19. The method of claim 16 wherein the encapsulant precursor materialcomprises sodium salicylate.
 20. The method of claim 16 wherein theencapsulant precursor material comprises tetraethylorthosilicate. 21.The method of claim 16 wherein the encapsulant precursor materialcomprises N-acetylcysteine.
 22. The method of claim 16 wherein theencapsulant precursor material comprises glutathione.
 23. A particlecomprising a first light sensitive area comprising a first lightsensitive material and a second light sensitive area comprising a secondlight sensitive material different than the first light sensitivematerial.
 24. The particle of claim 23 wherein: one of the first lightsensitive material and the second light sensitive material comprises aninorganic light sensitive material; and the other of the first lightsensitive material and the second light sensitive material comprises anorganic dye based light sensitive material.